mitochondrial encephalomyopathy การใช้

This syndrome is probably a familial form of mitochondrial encephalomyopathy.
It is also found in MERRF ( Myoclonic Epilepsy with Ragged Red Fibers ), a rare mitochondrial encephalomyopathy.
FASTKD2 has been linked to mitochondrial encephalomyopathy associated with cytochrome c oxidase deficiency ( mitochondrial complex IV deficiency ).
This mutation is associated with both CPEO and Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes ( MELAS ).
Variants of MT-ND3 are associated with Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes ( MELAS ), Leigh's syndrome ( LS ) and Leber's hereditary optic neuropathy ( LHON ).